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2. Ethyl acetate - Wikipedia

   en.wikipedia.org/wiki/Ethyl_acetate

   Ethyl acetate (systematically ethyl ethanoate, commonly abbreviated EtOAc, ETAC or EA) is the organic compound with the formula CH 3 CO 2 CH 2 CH 3, simplified to C 4 H 8 O 2.This flammable, colorless liquid has a characteristic sweet smell (similar to pear drops) and is used in glues, nail polish removers, and the decaffeination process of tea and coffee.

3. Ethyl acetate (data page) - Wikipedia

   en.wikipedia.org/wiki/Ethyl_acetate_(data_page)

   Download as PDF; Printable version; ... Gas properties Std enthalpy change ... for Ethyl Acetate/Ethanol [3] P = 760 mmHg BP Temp. °C

4. List of boiling and freezing information of solvents - Wikipedia

   en.wikipedia.org/wiki/List_of_boiling_and...

   This Wikipedia page provides a comprehensive list of boiling and freezing points for various solvents.

5. Solvent - Wikipedia

   en.wikipedia.org/wiki/Solvent

   A solvent dissolves a solute, resulting in a solution Ethyl acetate, a nail polish solvent. [1]A solvent (from the Latin solvō, "loosen, untie, solve") is a substance that dissolves a solute, resulting in a solution.

6. Azeotrope tables - Wikipedia

   en.wikipedia.org/wiki/Azeotrope_tables

   This page contains tables of azeotrope data for various binary and ternary mixtures of solvents. The data include the composition of a mixture by weight (in binary azeotropes, when only one fraction is given, it is the fraction of the second component), the boiling point (b.p.) of a component, the boiling point of a mixture, and the specific gravity of the mixture.

7. Acetic acid - Wikipedia

   en.wikipedia.org/wiki/Acetic_acid

   acetyl chloride SOCl 2 acetic acid (i) Li[AlH 4], ether (ii) H 3 O + ethanol Two typical organic reactions of acetic acid Acetic acid undergoes the typical chemical reactions of a carboxylic acid. Upon treatment with a standard base, it converts to metal acetate and water. With strong bases (e.g., organolithium reagents), it can be doubly deprotonated to give LiCH 2 COOLi. Reduction of acetic ...

8. Fischer–Speier esterification - Wikipedia

   en.wikipedia.org/wiki/Fischer–Speier...

   Over time, the acidity of the acetic acid and tannins in an aging wine will catalytically protonate other organic acids (including acetic acid itself), encouraging ethanol to react as a nucleophile. As a result, ethyl acetate—the ester of ethanol and acetic acid—is the most abundant ester in wines. Other combinations of organic alcohols ...

9. Acetylacetone - Wikipedia

   en.wikipedia.org/wiki/Acetylacetone

   The enzyme acetylacetone dioxygenase cleaves a central carbon-carbon bond of acetylacetone, producing acetate and 2-oxopropanal. The enzyme is iron(II)-dependent, but it has been proven to bind to zinc as well. Acetylacetone degradation has been characterized in the bacterium Acinetobacter johnsonii. [13] CH 3 C(O)CH 2 C(O)CH 3 + O 2 → CH 3 ...